US2002136736A1PendingUtilityA1

Papillomavirus L2 protein

52
Assignee: CANCER RES CAMPAIGN TECHPriority: Jun 26, 1991Filed: Jan 18, 2002Published: Sep 26, 2002
Est. expiryJun 26, 2011(expired)· nominal 20-yr term from priority
A61K 2039/552A61P 31/20A61P 35/00C12N 2710/20034A61K 38/00C07K 14/005A61K 39/12A61P 31/12C07K 2319/00A61K 2039/585C07K 2319/40C12N 7/00A61K 2039/70A61K 2039/55566C12N 2710/20022
52
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Claims

Abstract

The L2 protein of papillomavirus (particularly BPV-2 and BPV-4) has been cloned as a fusion protein with beta-galactosi-dase and GST; both as the whole protein and as fragments. Vaccination of calves is found to have both a prophylactic effect in tumor prevention and a therapeutic effect in tumor regression.

Claims

exact text as granted — not AI-modified
1 . A pharmaceutical formulation for the prophylaxis or therapy of papillomavirus tumours, which comprises papillomavirus L2 protein or prophylactically or therapeutically effective fragment thereof in admixture with a pharmaceutically acceptable carrier.  
     
     
         2 . A formulation according to  claim 1  wherein the L2 protein is a bovine papillomavirus BPV-2 protein or fragment thereof.  
     
     
         3 . A formulation according to  claim 2  wherein the L2 protein fragment comprises substantially amino acids 90 to 467.  
     
     
         4 . A formulation according to  claim 1  wherein the L2 protein is a bovine papillomavirus BPV-4 protein or fragment thereof.  
     
     
         5 . A formulation according to  claim 1  in the form of an injectable formulation, wherein the carrier is a pharmaceutically acceptable injection vehicle.  
     
     
         6 . A formulation according to  claim 5  which further comprises an adjuvant.  
     
     
         7 . A formulation according to  claim 1  wherein the L2 protein is present in the form of a fusion protein with a different co-protein.  
     
     
         8 . A formulation according to  claim 7  wherein the co-protein in the L2 fusion protein is beta-galactosidase.  
     
     
         9 . A formulation ac cording to  claim 7  wherein the co-protein is glutathione S-transferase (GST).  
     
     
         10 . A formulation according to  claim 1  which further comprises papillomavirus E7 protein or effective fragment thereof.  
     
     
         11 . A formulation according to  claim 1  wherein the L2 protein or fragment thereof is produced by recombinant DNA techniques.  
     
     
         12 . A transformed bacterial cell producing recombinant L2 protein or therapeutically effective fragment thereof.  
     
     
         13 . Use of papillomavirus L2 protein or effective fragment thereof in medicine for the prophylaxis or therapy of papillomavirus tumours.  
     
     
         14 . Use of papillomavirus L2 protein or therapeutically effective fragment thereof in the production of a medicament for use in the prophylaxis or therapy of papillomavirus tumours.  
     
     
         15 . A method of treating a mammal for the therapy of papillomavirus tumours, which comprises the administration of papillomavirus L2 protein or effective fragment thereof to the mammal in a prophylactically or therapeutically effective dosage.

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